ENST00000559133.6:c.*327T>C
|
ENSP00000453958.2:n.*327T>C
|
|
ENST00000674301.2:c.*1032T>C
|
ENSP00000501333.2:n.*1032T>C
|
|
ENST00000682170.1:n.1700T>C
|
|
|
ENST00000682767.1:n.816T>C
|
|
|
ENST00000316623.10:c.7519T>C
MANE Select
|
ENSP00000325527.5:p.Phe2507Leu
|
|
ENST00000674301.1:c.2685T>C
|
ENSP00000501333.1:n.2685T>C
|
|
ENST00000316623.9:c.7519T>C
|
ENSP00000325527.5:p.Phe2507Leu
|
|
ENST00000559133.5:c.2888T>C
|
|
|
NM_000138.4:c.7519T>C , LRG_778t1:c.7519T>C
|
NP_000129.3:p.Phe2507Leu
|
|
NM_000138.5:c.7519T>C
MANE Select
|
NP_000129.3:p.Phe2507Leu
|
|